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MSeqDR: A Centralized Knowledge Repository and Bioinformatics Web Resource to Facilitate Genomic Investigations in Mitochondrial Disease.
Shen, Lishuang; Diroma, Maria Angela; Gonzalez, Michael; Navarro-Gomez, Daniel; Leipzig, Jeremy; Lott, Marie T; van Oven, Mannis; Wallace, Douglas C; Muraresku, Colleen Clarke; Zolkipli-Cunningham, Zarazuela; Chinnery, Patrick F; Attimonelli, Marcella; Zuchner, Stephan; Falk, Marni J; Gai, Xiaowu.
Afiliación
  • Shen L; Center for Personalized Medicine, Children's Hospital Los Angeles, Los Angeles, California, USA.
  • Diroma MA; Massachusetts Eye and Ear Infirmary, Harvard Medical School, 243 Charles St, Boston, Massachusetts, USA.
  • Gonzalez M; Department of Biosciences, Biotechnologies and Biopharmaceutics, University of Bari, Bari, Italy.
  • Navarro-Gomez D; CEINGE-Biotecnologie Avanzate, Napoli, Italy.
  • Leipzig J; Dr. John T. Macdonald Foundation Department of Human Genetics, University of Miami Miller School of Medicine, Miami, Florida, USA.
  • Lott MT; The Genesis Project, Miami, Florida, USA.
  • van Oven M; Massachusetts Eye and Ear Infirmary, Harvard Medical School, 243 Charles St, Boston, Massachusetts, USA.
  • Wallace DC; Center for Biomedical Informatics, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Muraresku CC; Center for Mitochondrial and Epigenomic Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Zolkipli-Cunningham Z; Department of Forensic Molecular Biology, Erasmus MC - University Medical Center Rotterdam, The Netherlands.
  • Chinnery PF; Center for Mitochondrial and Epigenomic Medicine, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Attimonelli M; Department of Pathology, The Children's Hospital of Philadelphia and University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Zuchner S; Division of Human Genetics, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia USA.
  • Falk MJ; Division of Neurology, Department of Pediatrics, The Children's Hospital of Philadelphia, Philadelphia, USA.
  • Gai X; Department of Clinical Neurosciences, Cambridge Biomedical Campus, Cambridge, United Kingdom.
Hum Mutat ; 37(6): 540-548, 2016 06.
Article en En | MEDLINE | ID: mdl-26919060
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Biología Computacional / Enfermedades Mitocondriales / Bases de Datos Genéticas Límite: Humans Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Biología Computacional / Enfermedades Mitocondriales / Bases de Datos Genéticas Límite: Humans Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos